FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1003408005: Congenital dystrophy of cornea (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168182019 Congenital dystrophy of cornea (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168183012 Congenital corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168184018 Congenital dystrophy of cornea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168182019 Congenital dystrophy of cornea (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168183012 Congenital corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168184018 Congenital dystrophy of cornea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
511451000274119 Kongenitale Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
553831000274116 Kongenitale Dystrophie der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5847241000241117 dystrophie congénitale de la cornée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5847251000241119 dystrophie cornéenne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5847241000241117 dystrophie congénitale de la cornée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5847251000241119 dystrophie cornéenne congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
511451000274119 Kongenitale Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
553831000274116 Kongenitale Dystrophie der Kornea de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dystrophy of cornea (disorder) Is a Congenital structural abnormality of cornea true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophy of cornea (disorder) Is a Corneal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dystrophy of cornea (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophy of cornea (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophy of cornea (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital dystrophy of cornea (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Francois syndrome Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Stern Lubinsky Durrie syndrome (disorder) Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ophthalmomandibulomelic dysplasia Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital macular corneal dystrophy Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive, postlingual sensorineural hearing loss. Is a True Congenital dystrophy of cornea (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start